Hydrochloric Acid → 6-(Piperidin-4-ylamino)-4-trifluoromethyl-nicotinic acid methyl ester dihydrochloride

HRID 2355561ノート

反応式

HRID 2355561 の反応式
[CH3:1][O:2][C:3](=[O:28])[C:4]1[C:9]([C:10]([F:13])([F:12])[F:11])=[CH:8][C:7]([NH:14][CH:15]2[CH2:20][CH2:19][N:18](C(OC(C)(C)C)=O)[CH2:17][CH2:16]2)=[N:6][CH:5]=1.[ClH:29]>C1COCC1.O1CCOCC1>[ClH:29].[ClH:29].[CH3:1][O:2][C:3](=[O:28])[C:4]1[C:9]([C:10]([F:12])([F:13])[F:11])=[CH:8][C:7]([NH:14][CH:15]2[CH2:16][CH2:17][NH:18][CH2:19][CH2:20]2)=[N:6][CH:5]=1

参加物

5

反応物 2

HCID 313Hydrochloric AcidHCID 673987916-(1-tert-Butoxycarbonyl-piperidin-4-ylamino)-4-trifluoromethyl-nicotinic acid methyl ester

生成物 1

HCID 426042136-(Piperidin-4-ylamino)-4-trifluoromethyl-nicotinic acid methyl ester dihydrochloride

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 312751,4-Dioxane溶媒

実験手順

A solution of 6-(1-tert-butoxycarbonyl-piperidin-4-ylamino)-4-trifluoromethyl-nicotinic acid methyl ester (1.65 g, 4.09 mmol) in THF (10 mL) and 4 M HCl in dioxane (20 mL) was stirred at rt for 1 h. The solvent was removed under reduced pressure and the crude product used in the consecutive step without further purification assuming quantitative deprotection and formation of the dihydrochloride salt. MS (ISP): 304.0 [M+H]+.

後処理

  1. customThe solvent was removed under reduced pressure
  2. customthe crude product used in the consecutive step without further purification

出典と根拠

ORDレコード
ord-9ba3ccdd275240768139745232f5cdce
出典データセット
uspto-grants-2010_07
特許番号
US07754744B2

反応ノート

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